Adipose tissue cholesteryl ester transfer protein mRNA in response to probucol treatment: cholesterol and species dependence.

Probucol treatment results in an increase in plasma concentrations of cholesteryl ester transfer protein (CETP) which may account, in part, for the effects of this agent on plasma concentrations of HDL cholesterol. We have examined the mechanism by which probucol increases plasma CETP and have determined the associated changes in the plasma distribution of high density lipoprotein (HDL) particles. Studies were carried out in nine hypercholesterolemic subjects and five normal volunteers. Probucol treatment resulted in a 31% increase in plasma concentrations of CETP and a 23% decrease in HDL cholesterol (P < 0.01). The plasma concentration of LpA-I decreased by 40% (P < 0.01) whereas no change occurred in the LpA-I/A-II subclass of HDL. Plasma CETP increased significantly by 1 week of therapy and remained stable over 10 to 14 weeks of therapy. In spite of the significant increase in plasma concentrations of CETP, the abundance of CETP mRNA in peripheral adipose tissue decreased markedly (P < 0.001). These results suggested that probucol may alter CETP synthesis in another tissue such as liver or, alternatively, may have other effects on CETP secretion into or catabolism out of the plasma pool. Further studies were carried out in hamsters because, in this species, adipose tissue is a major site and liver is a negligible site for CETP synthesis. Hamsters were fed probucol with or without dietary cholesterol because this species was previously shown to respond to dietary cholesterol with an increase in adipose tissue mRNA levels and in plasma CETP concentrations, thus providing the opportunity to determine whether probucol would alter these parameters independently of the dietary cholesterol effect.(ABSTRACT TRUNCATED AT 250 WORDS)

[1]  A. Tall,et al.  Cholesteryl ester transfer protein and high density lipoprotein responses to cholesterol feeding in men: relationship to apolipoprotein E genotype. , 1993, Journal of lipid research.

[2]  A. Tall,et al.  Dietary cholesterol increases transcription of the human cholesteryl ester transfer protein gene in transgenic mice. Dependence on natural flanking sequences. , 1992, The Journal of clinical investigation.

[3]  P. Barter,et al.  Changes in the size of reconstituted high density lipoproteins during incubation with cholesteryl ester transfer protein: the role of apolipoproteins. , 1992, Journal of lipid research.

[4]  S. Yokoyama Cholesteryl ester transfer protein , 1991, The Lancet.

[5]  J. Breslow,et al.  Probucol decreases apolipoprotein A-I transport rate and increases high density lipoprotein cholesteryl ester fractional catabolic rate in control and human apolipoprotein A-I transgenic mice. , 1991, Arteriosclerosis and thrombosis : a journal of vascular biology.

[6]  R. Ulrich,et al.  Evidence that the nonparenchymal cells of the liver are the principal source of cholesteryl ester transfer protein in primates. , 1991, The Journal of biological chemistry.

[7]  A. Tall,et al.  Plasma concentrations of cholesteryl ester transfer protein in hyperlipoproteinemia. Relation to cholesteryl ester transfer protein activity and other lipoprotein variables. , 1991, Arteriosclerosis and thrombosis : a journal of vascular biology.

[8]  A. Tall,et al.  Reduced high density lipoprotein cholesterol in human cholesteryl ester transfer protein transgenic mice. , 1991, The Journal of biological chemistry.

[9]  S. Phinney,et al.  The transient hypercholesterolemia of major weight loss. , 1991, The American journal of clinical nutrition.

[10]  A. Tall,et al.  Plasma lipid transfer protein as a determinant of the atherogenicity of monkey plasma lipoproteins. , 1991, The Journal of clinical investigation.

[11]  A. Tall,et al.  Increase in plasma cholesteryl ester transfer protein during probucol treatment. Relation to changes in high density lipoprotein composition. , 1991, Arteriosclerosis and thrombosis : a journal of vascular biology.

[12]  A. Tall,et al.  Mammalian adipose tissue and muscle are major sources of lipid transfer protein mRNA. , 1991, The Journal of biological chemistry.

[13]  S. Yamashita,et al.  Accumulation of apolipoprotein E-rich high density lipoproteins in hyperalphalipoproteinemic human subjects with plasma cholesteryl ester transfer protein deficiency. , 1990, The Journal of clinical investigation.

[14]  J. Fruchart,et al.  Differential electroimmunoassay of human LpA-I lipoprotein particles on ready-to-use plates. , 1990, Clinical chemistry.

[15]  A. Tall,et al.  Atherogenic diet increases cholesteryl ester transfer protein messenger RNA levels in rabbit liver. , 1990, The Journal of clinical investigation.

[16]  A. Tall,et al.  Molecular basis of lipid transfer protein deficiency in a family with increased high-density lipoproteins , 1989, Nature.

[17]  V. Vaccarino,et al.  Mechanisms of HDL reduction after probucol. Changes in HDL subfractions and increased reverse cholesteryl ester transfer. , 1989, Arteriosclerosis.

[18]  P. Julien,et al.  Interactions of High Density Lipoprotein Subclasses (hdl2 and Hdlc) with Dog Adipocytes: Selective Effects of Cholesterol and Saturated Fat Feeding , 2022 .

[19]  P. Chomczyński,et al.  Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. , 1987, Analytical biochemistry.

[20]  J. Albers,et al.  Distribution and localization of lecithin:cholesterol acyltransferase and cholesteryl ester transfer activity in A-I-containing lipoproteins. , 1986, Journal of lipid research.

[21]  Roger A. Renfrew,et al.  Lipid Research Clinics Program. , 1984, JAMA.

[22]  D. Melton,et al.  Efficient in vitro synthesis of biologically active RNA and RNA hybridization probes from plasmids containing a bacteriophage SP6 promoter. , 1984, Nucleic acids research.

[23]  C. Packard,et al.  The hypolipidemic action of probucol: a study of its effects on high and low density lipoproteins. , 1983, Journal of lipid research.

[24]  Y. Marcel,et al.  Characterization of monoclonal antibodies against human apolipoprotein E. , 1981, The Journal of clinical investigation.

[25]  G. Bray,et al.  Synthesis of fatty acids and cholesterol by liver, adipose tissue and intestinal mucosa from obese and control patients , 1979, European journal of clinical investigation.

[26]  C. Rizzi Statistical Methods , 2020, Springer Theses.

[27]  W. Beltz,et al.  Evaluation of pathways for the cellular uptake of high density lipoprotein cholesterol esters in rabbits. , 1991, The Journal of clinical investigation.

[28]  A. Tall,et al.  Distribution and concentration of cholesteryl ester transfer protein in plasma of normolipemic subjects. , 1990, The Journal of clinical investigation.

[29]  A. Tall Plasma lipid transfer proteins. , 1986, Journal of lipid research.